Genes | GeDiPNet - Gene Disease Pathway & Associations

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Showing genes starting with "C"

1171 to 1180 of 1338 Genes

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	Entrez ID	Gene Symbol	Gene Name	Synonyms	Diseases
1171	85301	COL27A1	Collagen type XXVII alpha 1 chain	STLS	Desbuquois syndrome, Osteoarthritis, Tourette syndrome, Diabetes mellitus, type 2
1172	8532	CPZ	Carboxypeptidase Z	-	Neuroblastoma
1173	8536	CAMK1	Calcium/calmodulin dependent protein kinase I	CAMKI
1174	85417	CCNB3	Cyclin B3	CYCB3	Osteosarcoma
1175	85445	CNTNAP4	Contactin associated protein family member 4	CASPR4	Alzheimer disease, Hepatocellular carcinoma, Color vision deficiency, Melanoma, Prostate cancer
1176	8556	CDC14A	Cell division cycle 14A	DFNB105, DFNB32, DFNB35, cdc14, hCDC14	Isolated sensorineural deafness, Nonsyndromic hearing loss, Breast cancer, Deafness, Hearing impairment, Hearing loss, Male infertility, Male reproductive organ cancer
1177	8558	CDK10	Cyclin dependent kinase 10	ALSAS, PISSLRE	Al kaissi syndrome, Attention deficit hyperactivity disorder, Autism, Bipolar disorder, Melanoma, Global developmental delay, Major depressive disorder, Schizophrenia
1178	857	CAV1	Caveolin 1	BSCL3, CGL3, LCCNS, MSTP085, PPH3, VIP21	Amyotrophic lateral sclerosis, Atrial fibrillation, Atrial flutter, Breast neoplasm, Carcinogenesis, Basal cell carcinoma, Ovarian carcinoma, Cardiac arrhythmia, Cardioembolic stroke, Cardiomegaly, Experimental diabetes, Diffuse cutaneous systemic sclerosis, Generalized lipodystrophy, Partial lipodystrophy, Pulmonary hypertension View all (19 more)
1179	8573	CASK	Calcium/calmodulin dependent serine protein kinase	CAGH39, CAMGUK, CMG, FGS4, LIN2, MICPCH, MRXSNA, TNRC8, hCASK	Congenital nonspherocytic hemolytic anemia, Carcinoma, Cerebellar diseases, Cerebellar hypoplasia/atrophy, epilepsy, and global developmental delay, Congenital brain malformation, Congenital microcephaly, Congenital neurologic anomalies�, Developmental disability, Developmental and epileptic encephalopathy, Global developmental delay, Hydranencephaly, Intellectual developmental disorder microcephaly cerebellar, Intellectual developmental disorder, x-linked, Intellectual developmental disorder, Lissencephaly View all (8 more)
1180	858	CAV2	Caveolin 2	CAV	Amyotrophic lateral sclerosis, Rheumatoid arthritis, Atrial fibrillation, Cardiac arrhythmia, Cardiac embolism, Cardioembolic stroke, Glaucoma, Open angle glaucoma, Pancreatic cancer, Prostatic neoplasm, Uterine fibroid

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